Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011872Generated: November 2, 2026

Cesium carbonate → 3,5-Dimethyl-1-(5-trifluoromethyl-pyridin-3-yl)-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1011872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactantethyl 3,5-dimethyl-1H-pyrazole-4-carboxylateHCID 215436—
Reactant3-Bromo-5-(trifluoromethyl)pyridineHCID 11127991—
CatalystCopper iodideHCID 83717—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
Product3,5-Dimethyl-1-(5-trifluoromethyl-pyridin-3-yl)-1H-pyrazole-4-carboxylic acid ethyl esterHCID 6731458835%

Reaction Conditions

Temperature160 °C

Reaction Steps

3,5-Dimethyl-1H-pyrazole-4-carboxylic acid ethyl ester (0.10 g, 1 mmol) (prepared as described in Tett 2002, 58, 18, p 3639), 3-bromo-5-trifluoromethyl-pyridine (0.16 g, 1 mmol), copper iodide (0.02 g, 0.2 mmol) and cesium carbonate (1.0 g, 3 mmol) were suspended in DMA (0.5 ml) and heated to 160° C. for 16 h. The reaction was diluted with EtOAc, washed repeatedly with ammonium hydroxide, brine and dried (Na2SO4) and concentrated. The residue was purified by flash column chromatography (EtOAc:n-heptane 1:9-2:8 gradient affording the title compound (0.07 g, 35%) as a yellow oil. MS: 314.2 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977358B2
Source datasetuspto-grants-2011_07
ORD IDord-9eef111c3cb747368e7f36c2210fabc2
Source noteuspto-grants-2011_07